Article
Mutations in CHMP2B are not a cause of frontotemporal lobar degeneration in Finnish patients.
European journal of neurology - 1 Nov 2010
Kaivorinne A-L, Krüger J, Udd B, Majamaa K, Remes A M
Abstract excerpt
BACKGROUND: Frontotemporal lobar degeneration (FTLD) is a genetically complex disorder. The majority of mutations linked to FTLD families are found in the microtubule-associated protein tau (MAPT) and progranulin (PGRN) genes. Mutations in the chromatin-modifying protein 2B gene (CHMP2B) have bee...
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